4.5 Article

Structural dynamics bridge the gap between the genetic and functional levels of GPCRs

期刊

CURRENT OPINION IN STRUCTURAL BIOLOGY
卷 69, 期 -, 页码 150-159

出版社

CURRENT BIOLOGY LTD
DOI: 10.1016/j.sbi.2021.04.005

关键词

Receptor signaling; GPCRs; Structural dynamics; Web resources; Computational biology

资金

  1. Spanish Ministry of Science, Innovation and Universities [FPU16/01209]
  2. National Center of Science, Poland [2017/27/N/NZ2/02571]
  3. Lundbeck foundation [R163-2013-16327]
  4. Novo Nordisk Foundation [NNF18OC0031226]
  5. Instituto de Salud Carlos III FEDER [PI15/00460, PI18/00094]
  6. ERA-NET NEURON & Ministry of Economy, Industry and Competitiveness [AC18/00030]

向作者/读者索取更多资源

G protein-coupled receptors are crucial in human physiological processes and are affected by genetic encoding and sequence diversity. Understanding the link between protein sequence, structure, and function is essential for interpreting the physiological response of GPCRs.
G protein-coupled receptors (GPCRs) are implicated in nearly all physiological processes in the human body and represent an important drug targeting class. The genes encoding the different GPCR (sub)types determine their specific functionality, which can be altered by natural genetic variants and isoforms. Deciphering the molecular link between sequence diversity and its functional consequences is a current challenge and critical for the comprehension of the physiological response of GPCRs. It requires a global understanding of how protein sequence translates into protein structure, how this impacts the structural motions of the protein, and, finally, how all these factors determine the receptor functionality. Here, we discuss available resources and state-of-the-art computational approaches to address this question.

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